The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
109488963 10948896 3 F 201307 20160627 20150324 20160712 PER US-PFIZER INC-2015097394 PFIZER 55.00 YR F Y 77.00000 KG 20160712 OT US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
109488963 10948896 1 PS LYRICA PREGABALIN 1 150 MG, 2X/DAY U 21446 150 MG CAPSULE, HARD BID
109488963 10948896 2 SS LYRICA PREGABALIN 1 Oral 100 MG, 2X/DAY U 21446 100 MG CAPSULE, HARD BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109488963 10948896 1 Fibromyalgia
109488963 10948896 2 Dysaesthesia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
109488963 10948896 Arthralgia
109488963 10948896 Burning sensation
109488963 10948896 Gait disturbance
109488963 10948896 Hypoaesthesia
109488963 10948896 Paraesthesia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
109488963 10948896 1 2013 0